Abstract:In this work, an effective approach to synthesize large-area Cu(2)S hierarchical nanotree arrays is presented: Cu nanowire arrays synthesized via template-assisted electrodeposition are used as precursors for the self-growth of branched Cu(2)S nanotree arrays by a gas-solid reaction in H(2)S atmosphere at room temperature. The branched Cu(2)S nanotrees with a high aspect ratio are vertically aligned over the Au film surface, forming a nanoscale 'forest'. Electron microscopy studies reveal that the treelike bra… Show more
“…The excitation wavelength is 514.5 nm from an Ar ion laser. A strong and sharp band at 472 cm -1 probably originates from the lattice vibration, which is consistent with the results reported for Cu 2 S films
[41,42] and Cu 2 S nanotree arrays
[43]. …”
A versatile, low-temperature, and low-cost chemical conversion synthesis has been developed to prepare copper sulfide (Cu2S) nanotubes. The successful chemical conversion from ZnS nanotubes to Cu2S ones profits by the large difference in solubility between ZnS and Cu2S. The morphology, structure, and composition of the yielded products have been examined by field-emission scanning electron microscopy, transmission electron microscopy, and X-ray diffraction measurements. We have further successfully employed the obtained Cu2S nanotubes as counter electrodes in dye-sensitized solar cells. The light-to-electricity conversion results show that the Cu2S nanostructures exhibit high photovoltaic conversion efficiency due to the increased surface area and the good electrocatalytical activity of Cu2S. The present chemical route provides a simple way to synthesize Cu2S nanotubes with a high surface area for nanodevice applications.
“…The excitation wavelength is 514.5 nm from an Ar ion laser. A strong and sharp band at 472 cm -1 probably originates from the lattice vibration, which is consistent with the results reported for Cu 2 S films
[41,42] and Cu 2 S nanotree arrays
[43]. …”
A versatile, low-temperature, and low-cost chemical conversion synthesis has been developed to prepare copper sulfide (Cu2S) nanotubes. The successful chemical conversion from ZnS nanotubes to Cu2S ones profits by the large difference in solubility between ZnS and Cu2S. The morphology, structure, and composition of the yielded products have been examined by field-emission scanning electron microscopy, transmission electron microscopy, and X-ray diffraction measurements. We have further successfully employed the obtained Cu2S nanotubes as counter electrodes in dye-sensitized solar cells. The light-to-electricity conversion results show that the Cu2S nanostructures exhibit high photovoltaic conversion efficiency due to the increased surface area and the good electrocatalytical activity of Cu2S. The present chemical route provides a simple way to synthesize Cu2S nanotubes with a high surface area for nanodevice applications.
“…The result showed that cooling by water was necessary and very important in the experiment (Figure S3, Supporting Information). If the cooling was not employed or the cooling rate was slow, there would be some corroded films (as shown in Figures S2a and S3, Supporting Information) which should result from the thermal instability of the Cu 2− x S. The obtained nanosheets ( Figure a) were triangular with obvious Raman peak at 471 cm −1 (Figure b), which was consistent with the reported results of Cu 2 S films . The uniform Raman peak intensity mapping at 471 cm −1 showed that the specimen had pure β phase at room temperature (inset of Figure b).…”
2D triangular β-Cu S nanosheets with large size and high quality are synthesized by a novel method of super-cooling chemical-vapor-deposition. The phase transition of this 2D material from β-Cu S to γ-Cu S occurs at 258 K (-15 °C), and such transition temperature is 120 K lower than that of its bulk counterpart (about 378 K).
“…23 Among these the electrochemical synthesis of nanomaterials and thin lms could be a cost effective technology for the production of photoelectrochemical cell. Lai et al 27 have reported the template-assisted electrochemical synthesis of Cu 2 S nanowires where copper deposition occurred into the pores of an anodic aluminum oxide. The rationale for this is that thin lms modules are expected to be cheaper in manufacture owing to their low materials cost, energy consumption and handling cost.…”
Electrosynthesis of p-Cu 2 S thin films on a fluorine-doped tin oxide coated transparent conducting TCO (SnO 2 :F) glass substrate is carried out by chronoamperometry and cyclic voltammetry (CV) using an ethanolic solution of a single-source precursor (SP), [Cu(mdpa) 2 ][CuCl 2 ] (where mdpa is 3,5-dimethyl pyrazole-1-dithioic acid). The appropriate potential at which the formation of stoichiometric p-Cu 2 S thin films occurs was found to be À0.48 V. The mechanism of the selective deposition of the p-Cu 2 S phase can be described by the electroreduction of Cu-N/S bonds in the coordination sphere following the dissociation of a precursor complex into Cu + and mdpa. The free ligand mdpa is reduced to sulfide ion producing volatile organics in the electrochemical process. The quality deposition of thin films depends on the optimization of the SP concentration. An X-ray diffraction study reveals the high chalcosite phase of copper sulfide with preferential orientation along the (110) plane. The I-V characteristic of the as deposited Cu 2 S/TCO thin film shows a non-ohmic behavior suggesting the formation of a p-n heterojunction diode. The p-Cu 2 S/TCO thin films are found to be excellent photocatalysts for the photo-degradation of Congo Red (CR) under visible light irradiation. It has also been shown that the photocatalytic activity of the deposited thin films increased many fold with the addition of a catalytic amount of hydrogen peroxide in the photo-degradation of Rose Bengal (RB) dye under visible light irradiation. A possible mechanism for the improved photoactivity of p-Cu 2 S/TCO is proposed and involves the electron scavenging property of H 2 O 2 followed by OH À radical formation, significantly accelerating the photodegradation of RB dye.
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